Searching journal content for articles similar to Mihola et al. 29 (7): 1078.

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  1. ...encyclopedia of DNA elements in the human . Nature 489: 57–74. ↵Eram MS, Bustos SP, Lima-Fernandes E, Siarheyeva A, Senisterra G, Hajian T, Chau I, Duan S, Wu H, Dombrovski L, et al. 2014. Trimethylation of histone H3 lysine 36 by human methyltransferase PRDM9 protein. J Biol Chem 289: 12177...
  2. ...of the experimental data sets.For each hotspot, we also inferred the fraction of reads that originated from the B6 and the CAST chromosomes respectively, as previously described (Davies et al. 2016). PRDM9 has a histone methyltransferase activity, and binding to its target sites is associated with trimethylation of H...
  3. .... cerevisiae, these hotspots are not preferentially located in promoter regions, but they are enriched in H3K4me3 (Buard et al. 2009; Smagulova et al. 2011), presumably through PRDM9 methyltransferase activity (Hayashi et al. 2005). Indeed, PRDM9 can methylate histone H3 at K4, K9, and K36 in vitro (Wu et al...
  4. .... Their locations are predominantly determined by the zinc finger protein PRDM9, which binds to DNA in hotspots and subsequently uses its SET domain to locally trimethylate histone H3 at lysine 4 (H3K4me3). This sets the stage for double-strand break (DSB) formation and reciprocal exchange of DNA between chromatids...
  5. ...PRDM9 allelic forms of involvement in the development of preleukemic clones in B-ALL patients andwe propose that PRDM9histoneH3K4 methyltransferase activity in the parental germline could lead to the genomic instability associated with childhood ALL, a plausible mechanismconsistent with the current...
  6. ...and inactive in dogs. Axelsson et al. 58 Genome Research www..org Recombination initiation in dogs The PRDM9 protein contains a SET methyltransferase domain, which induces a histonemodification in the vicinity of a sequence motif bound by a zinc finger domain. This modification serves as a mark...
  7. ...events are mainly restricted to regions that contain specific motifs that act as binding sites for the PR/SET domain 9 (PRDM9) protein that marks regions for double-stranded breaks, which are repaired by recombination during meiosis (Baudat et al. 2010; Myers et al. 2010; Parvanov et al. 2010). Species...
  8. ...-mediated repression allows activation of ERV enhancers upon entry into meiosis. This regulatory feature is observed for independently evolved KZFPs and ERVs in mice and humans, suggesting evolutionary conservation in mammals. Further, we show that KZFP-targeted ERVs are underrepresented on the sex chromosomes...
  9. ..., calculated for ES cell and meiotic data sets. Elevated RNAPII occupancy during meiosis appears to be associated with increased DSB formation (black arrow). (E) Overlap of ChromHMM histone annotations with PRDM9 sites. Note DSB-favored sites are depleted for unmarked chromatin while enriched for H3K36me3...
  10. ...histone H3K4me3 and H3K36me3 (Mihola et al. 2009; Baudat et al. 2010; Myers et al. 2010; Parvanov et al. 2010; Grey et al. 2011, 2017; Brick et al. 2012; Lange et al. 2016; Powers et al. 2016). As a consequence, PRDM9-dependent SPO11 hotspots occur in nucleosome-depleted regions with well...
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